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- Tasks: Manage site activities and monitor oncology studies from home.
- Company: Parexel is a leader in clinical research, partnering with top biotechs and pharma companies.
- Benefits: Enjoy remote work, job security, and opportunities for career growth.
- Why this job: Be part of vital drug development while maintaining a healthy work-life balance.
- Qualifications: Experience in site management and oncology trials is preferred; strong organisational skills are essential.
- Other info: Join a supportive team and explore diverse career paths within Parexel.
The predicted salary is between 36000 - 60000 £ per year.
Parexel is currently seeking Clinical Research Associates, ideally with oncology experience, based in North England.
This will be a home-based position and fully dedicated to a single sponsor.
Working as a Clinical Research Associate at Parexel offers tremendous long-term job security and prospects. We undertake vital clinical studies for sponsors including the leading global biotechs and Pharma top 50. And we have an incredible pipeline of work.
Whether you see your future path as a CRA, or in fields such as clinical operations, project management, line management, or other positions, we have a world of opportunity waiting for you.
Our CRAs work from their home office base, supporting studies within their country or region. ‘Manageable sites, manageable protocols’ is our mantra. Expect exciting professional challenges in inspiring studies, but with time for your outside life.
Some specifics about this advertised role
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Dedicated to one client.
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Responsible for all site management and monitoring activities across assigned oncology studies
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Work with industry leaders and subject matter experts.
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Opportunity to mentor junior CRAs.
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Work with world-class technology.
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A pivotal role in the drug development process.
Here are a few requirements specific to this advertised role.
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Substantial Site Management experience, with an understanding of the clinical
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Trial methodology and terminology.
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Experience in, or willingness to monitor oncology clinical trials.
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Experience in independent monitoring, all types of visits.
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Effective time management, organizational and interpersonal skills & problem-solving skills, with the ability to multi-task and prioritize.
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Good understanding and working knowledge of clinical research, phases of clinical trials, current GCP/ICH & country clinical research law & guidelines.
We care about our people and your passion, as they are the key to our success, and provide an open and friendly work environment where we empower people and provide them with opportunities to develop their long-term careers. In addition, you will have the opportunity to develop within your role and tackle further responsibilities or develop your skill set within other related departments of Parexel.
Who are Parexel
Parexel supports clinical studies across the full range of therapeutic areas, and we have longstanding partnerships with a vast client base.
We supported the trials of most of today’s top 50 best-selling drugs, but equally we enable more niche drug developments that are critical to the well-being of many patients.
You’ll be an influential member of the wider team.
Not quite the role for you?
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Clinical Research Associate II (Oncology Experience) - Northern England, UK Remote - FSP employer: Parexel International
Contact Detail:
Parexel International Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Research Associate II (Oncology Experience) - Northern England, UK Remote - FSP
✨Tip Number 1
Familiarise yourself with the latest oncology clinical trial methodologies and terminology. This will not only boost your confidence during interviews but also demonstrate your commitment to the field, making you a more attractive candidate.
✨Tip Number 2
Network with current or former Clinical Research Associates at Parexel or similar companies. Engaging in conversations about their experiences can provide valuable insights into the role and help you tailor your approach when discussing your fit for the position.
✨Tip Number 3
Showcase your time management and organisational skills by preparing examples of how you've successfully managed multiple projects or tasks in the past. Being able to articulate these experiences will highlight your ability to thrive in a remote working environment.
✨Tip Number 4
Stay updated on the latest developments in GCP/ICH guidelines and country-specific clinical research laws. This knowledge will not only prepare you for potential interview questions but also demonstrate your proactive approach to staying informed in the ever-evolving field of clinical research.
We think you need these skills to ace Clinical Research Associate II (Oncology Experience) - Northern England, UK Remote - FSP
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in clinical research, particularly in oncology. Use specific examples of your site management and monitoring activities to demonstrate your expertise.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for clinical research and your understanding of the oncology field. Mention why you are interested in working with Parexel and how your skills align with their needs.
Highlight Relevant Skills: In your application, emphasise your time management, organisational, and problem-solving skills. Provide examples of how you've successfully managed multiple tasks or projects in previous roles.
Showcase Continuous Learning: Mention any ongoing education or training related to clinical trials, GCP/ICH guidelines, or oncology. This demonstrates your commitment to professional development and staying current in the field.
How to prepare for a job interview at Parexel International
✨Showcase Your Oncology Knowledge
Make sure to highlight any specific experience you have in oncology clinical trials. Be prepared to discuss relevant studies you've worked on and how they relate to the role at Parexel.
✨Demonstrate Site Management Skills
Since the role requires substantial site management experience, come ready to share examples of how you've effectively managed sites in previous roles. Discuss your approach to problem-solving and time management.
✨Familiarise Yourself with GCP/ICH Guidelines
Brush up on Good Clinical Practice (GCP) and International Council for Harmonisation (ICH) guidelines. Being able to discuss these regulations confidently will show your understanding of the clinical research landscape.
✨Prepare Questions for the Interviewers
Think of insightful questions to ask about the company culture, team dynamics, and opportunities for professional development. This shows your genuine interest in the role and helps you assess if it's the right fit for you.